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HS Code |
205176 |
| Product Name | 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride |
| Cas Number | 142350-50-1 |
| Molecular Formula | C12H15ClF3N |
| Molecular Weight | 265.70 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Melting Point | 173-177°C |
| Solubility | Soluble in water and DMSO |
| Storage Conditions | Store at 2-8°C |
| Synonyms | 1-(3-(Trifluoromethyl)phenyl)piperidine hydrochloride |
| Chemical Class | Aromatic piperidine derivative |
As an accredited 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is packaged in a 25g amber glass bottle, sealed, labeled with the chemical name, CAS number, and safety information. |
| Shipping | 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride is securely packaged in sealed, clearly labeled containers to ensure stability and prevent contamination. The chemical is shipped in compliance with all relevant safety regulations, accompanied by proper documentation and handling instructions. Temperature-controlled shipping is available if required to maintain product integrity during transit. |
| Storage | 4-(3-Trifluoromethylphenyl)piperidine hydrochloride should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Store at room temperature or as recommended by the manufacturer. Keep away from incompatible materials such as strong oxidizing agents. Ensure proper labeling and secure storage to prevent unauthorized access and accidental release. |
Applications of 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride in Industrial Manufacturing4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride serves as a specialized intermediate in highly regulated synthetic processes across pharmaceutical and fine chemical industries. Drawing from our in-plant technical records and validated customer use cases, the following outlines core downstream applications where this raw material contributes to scalable and compliant production, detailing domain-specific compliance requirements, formulation approaches, integrated process stages, and finished product profiles. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisThis compound functions as a critical structural fragment in the multi-step synthesis of next-generation central nervous system (CNS) pharmaceuticals. Our manufacturing customers implement it in batch and continuous flow systems, responding precisely to quality and purity demands from reference and generic drug production pipelines targeting neuropsychiatric and analgesic compounds. Secure supply of this building block supports both patent-protected molecule innovation and commercial-scale API output, with clear traceability and in-process monitoring for regulatory inspection readiness. Industry compliance standards
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2. Advanced Agrochemical Intermediate ManufacturingThis raw material enters agrochemical research and industrial synthesis chains as an intermediate for novel crop protection actives. Leading agrochemical companies utilize it in developing selective herbicides and insecticides where fluorinated piperidine motifs offer distinct environmental stability and target specificity. The ingredient plays a role in pre-commercial synthesis campaigns and scaling to technical-grade products, with batch records tightly aligned to both local and export regulatory requirements. Industry compliance standards
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3. Custom Synthesis for Medicinal Chemistry Building BlocksContract research organizations (CROs) and medicinal chemistry labs integrate this material for the assembly of high-value fluorinated scaffolds needed in preclinical candidate libraries. The piperidine core’s trifluoromethyl substitution enhances metabolic stability and target binding for SAR (structure–activity relationship) studies. Shipments fulfill stringent customer specs and are accompanied by full batch analytics, supporting regulatory documentation for submission to oversight agencies during stage-gated research and IND-enabling studies. Industry compliance standards
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4. Fine Chemical Synthesis for Specialty Material PrecursorsIn the fine chemicals sector, formulators use this compound as a tailored precursor for specialty monomer and polymer applications, particularly when increased fluorine content is required for membrane or coating durability. Integration into cross-coupling or functionalization lines enables the formation of high-purity intermediates destined for further processing in electronics-grade and advanced material production. Product traceability and in-process impurity control are prioritized to meet advanced technical specification sheets for these industries. Industry compliance standards
Typical usage ratio
Downstream process integration
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Some chemical ingredients wind up in our hands through years of listening to researchers and formulators describe exactly what’s missing from commercial libraries. 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride is a good example. This compound first gained attention for its performance in medicinal chemistry and fine chemical synthesis, and that has shaped the way we continue to refine our process. We stick to pharmaceutical-grade synthesis and purification because we work with teams that count on the kind of lot-to-lot consistency that only careful in-house work can deliver. Every batch that leaves our plant represents weeks of control, analysis, and documentation that a lot of smaller operations simply can’t sustain.
Any practical chemist will tell you that the real difference between two similar molecules comes out in the way they behave during real-world procedures. 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride isn’t just a piperidine salt with a trifluoromethyl twist. Our process brings together modern fluorination technology with robust plant-scale amination, yielding a product with high purity and reliable flow properties. Over time, we’ve fine-tuned our isolation steps to provide a white crystalline solid that meets the strictest specifications for residual solvents and byproducts. This isn’t just a theoretical benefit—it means fewer surprises in downstream processes for formulation teams.
Scaling up isn’t about just turning up the dials. The way a pilot batch behaves rarely maps perfectly onto industrial reactors, so our engineers pay close attention to cooling rates, crystallization, and filtration layouts. Every challenge—whether an unexpected exotherm or persistent emulsion—pushes us to refine our method further. Several years back, increasing demand from pharmaceutical development teams led us to add new monitoring steps. We adopted advanced analytical tools for intermediate testing, not just for the final product. This allowed better control over impurities, particularly fluorinated ones, which can complicate synthesis if left unchecked.
We pay special attention to particle size because our partners tell us about issues in tablet pressing and solution preparation. Too fine a fraction, and dusting becomes an issue; too coarse, and solubility suffers. We use controlled milling instead of generic grinding—a difference that really shows in processability. As for hydrochloride content, we keep our verification steps tight since even a few tenths of a percent matter for stoichiometry in scale-up synthesis. Most batches are colorless to faintly off-white, free from visible contamination and packed in lined containers that prevent atmospheric uptake. Every container leaves here with a full spectral profile, a lot record, and a promise of traceability.
Over several years, we’ve seen 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride play roles ranging from small-scale analog production to gram-scale syntheses of active pharmaceutical ingredients. Researchers appreciate the way this intermediate speeds up the formation of diaryl piperidine scaffolds, especially when exploring CNS active compounds. The trifluoromethyl group brings not just bulk, but also metabolic stability—a feature that carries through from lead optimization to pre-clinical studies. During collaborations with academic teams, we frequently field requests for custom packing, special purity grades, or assistance troubleshooting side reactions related to the hydrochloride handling. These interactions help us build protocols that work across a range of end uses, not just under ideal lab conditions.
Many in the field are familiar with 4-phenylpiperidine hydrochloride and its close cousins, so it’s natural to wonder what sets this compound apart. The introduction of a trifluoromethyl group at the meta-position confers chemical and physical effects beyond what simple phenyl substitutions offer. Solubility in certain protic solvents often increases, and the electron-withdrawing capacity shifts reactivity in arylation and cross-coupling reactions. During scale-up of certain intermediates, we see more favorable crystallization habits compared to non-fluorinated analogs, which reduces purification headaches. Initially, adoption faced some cost constraints—fluorinated building blocks traditionally came at a premium due to supply chain limitations. Our team invested in fluorine-handling infrastructure, which reduced both per-kilogram costs and order lead times.
No one enjoys the surprise of a degraded intermediate. Our storage recommendations come from years of real-world shipment and warehouse experience: we keep photo-sensitive and hygroscopic effects in mind. Each batch ships in triple-sealed containers with desiccant packs, and we train logistics partners to handle the material as they would a sensitive API precursor. While regulations regarding controlled substances grow stricter every year, our product consistently meets requirements for clean documentation and safe transit. When customers run into shelf-life concerns, we supply batch histories and can even do accelerated stability testing to support regulatory submissions.
Chemists developing new drug candidates or diagnostic reagents often face setbacks not because their route fails, but because intermediates behave unexpectedly. Whether it’s incompatibility with a chosen solvent, poor recovery rates due to deliquescence, or insoluble byproducts, a poorly manufactured intermediate can add weeks of troubleshooting. We gain valuable feedback from users after every delivery, and this shapes tweaks to our drying and purification steps. About two years ago, a customer pointed out minor issues with particle agglomeration during their automated dosing process. Instead of offering a stock response, our production team reviewed sieving protocols, eventually introducing a screening step to minimize clumping without over-milling the product.
Old habits in chemical procurement die hard. Many buyers look for the quick solution—buy the cheapest lot from a new source, hope for the best, fix bugs as they appear. Our experience teaches us that instability or hidden impurities in an intermediate add up to lost time and money downstream. Every time a customer switches to our material, they tell us about improved batch yields or better crystallization outcomes. We do this through transparency. Every lot is traceable back to specific raw material batches, with full analytical data from NMR, IR, and HPLC as standard release criteria. We don’t cut corners on documentation or replace technical support with generic email responses. Clients can always track a shipment to its origins and get real answers to technical questions, not canned responses or vague reassurances.
Commercial and academic labs alike operate in a world of shrinking budgets and rising expectations. Developing a new small molecule, especially for therapeutic use, involves hundreds of decisions where a failed reaction or unexplained impurity can sink an entire project. Good material supply means less unplanned downtime and more reproducible results. Our rigorous handling protocols and persistent quality controls translate to fewer analytical surprises mid-synthesis, which matters for customers pursuing regulatory filings or large-scale manufacturing. We recognize the risk faced by research teams and make it part of our mission to remove the supply-side hassle, one order at a time.
Process improvement doesn’t happen in a vacuum. Direct feedback from scientists, analysts, and production chemists shapes new batches as much as advances in synthetic methodology. Over years in this business, we’ve learned not to dismiss “minor” issues like end-of-lot weight discrepancies or subtle color shifts. Our plant features small-scale glassware as well as kilo-lab reactors, letting us test modifications before committing to full-scale changes. Unexpected precipitation, slow filtration, or unanticipated polymorph appearance have all provided valuable learning opportunities, ultimately strengthening our offering. The goal is not just to sell product, but to push the baseline for what this intermediate offers in the market.
Fluorochemicals demand careful sourcing due to specialized upstream requirements. We have established relationships with raw material suppliers who share our standards. Direct audits, spot checks, and analytical verification all play a part in keeping inbound materials in check. Years ago, difficulties with inconsistent trifluoromethylbenzene led our sourcing team to work alongside producers, reviewing purification techniques and advocating for pre-shipment analyses. The reward was not just traceable supply, but dependable batch outcomes even as the global market tightened. We take pride in lean but robust inventory management, backed by raw material traceability and real-time tracking.
Progress in the chemical sciences is measured at the bench, not just in boardrooms or by quarterly reports. Much of the credit for today’s advances in pharmaceutical design or agrochemical synthesis belongs to teams working under pressure, solving problems molecule by molecule. Our role, as we see it, is to meet them with materials supported by solid data, honest communication, and a willingness to adjust as projects unfold. Whether a customer works in process development, analytical method creation, or high-throughput screening, we listen closely. Product improvements often start with a single conversation about how something crystallizes, dissolves, or tolerates storage under challenging conditions. That kind of information exchange helps us deliver better compounds year after year.
Many of our customers work with agencies that demand more than just a certificate. They require analytical support, batch-specific documentation, and sometimes even custom studies for process validation. The audit process can be nerve-wracking, so we work to provide clean lot histories, up-to-date chromatographic records, and supplementary analytical services when requested. Our experience tells us that demonstrating control over critical attributes like water content, residual solvents, and trace impurities builds trust with both users and regulatory reviewers. By constantly updating our analytical suite and training staff in the latest techniques, we make it easier for our partners to move from bench to plant to client site with confidence.
Quality in specialty chemical manufacturing always reveals itself in use. We encourage users to share not just satisfactory analytic reports but practical insights: solubility drops, flowability concerns, reactivity issues, or unexpected side reactions. These are real world factors that impact timelines and decision-making. Through hundreds of kilo-scale and pilot-scale runs, occasional roadblocks surface. Overcoming these informs better screening, improved drying cycles, or even small shifts in crystal habit—each change rooted in feedback from chemists who rely on prompt deliveries and guaranteed performance. This commitment to ongoing improvement sets our 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride apart from bulk commodity options.
Any chemical can be sourced from a catalogue. Few suppliers stay engaged with a product long after it ships. We see ourselves as a manufacturing partner, not just a box on a shelf. Our lines stay open for technical support, repeat orders, and shared problem-solving. Adjustments to process, scale, or packaging often stem from partnership, not disconnect. Our goal is to keep 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride performing as not just another intermediate, but as a trusted component in more advanced applications. We invest in upgrading production lines, extending stability studies, and supporting custom synthesis requests so scientists can keep pushing the boundaries of their work.
Every kilogram of this compound that leaves our facility benefits from a history of listening, learning, and persistent effort to fix overlooked pain points. Our plant teams care as much about a compound’s fate in the workflow as in the warehouse. That attention translates to fewer setbacks in development and shorter cycles between iterations. This model, built on close collaboration with practicing chemists, gives our 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride real utility for anyone who wants reliable building blocks, not just more paperwork.
Chemical manufacturing never stands still. End uses for advanced intermediates like this one evolve faster than any single supplier can predict. Our team stays in close contact with the research and production communities who know this molecule best. We take suggestions for next-generation handling, alternative packaging, or even support for emerging analytical techniques seriously. Each batch begins as a synthesis, but the value emerges in the data, reports, and real-world performance from labs putting molecules to work. By staying open, detailed, and responsive, we aim to keep 4-(3-Trifluoromethylphenyl)Piperidine Hydrochloride a step ahead, meeting both today’s rigorous benchmarks and tomorrow’s creative chemical challenges.